J. Philpot

958 total citations
15 papers, 696 citations indexed

About

J. Philpot is a scholar working on Molecular Biology, Cell Biology and Immunology and Allergy. According to data from OpenAlex, J. Philpot has authored 15 papers receiving a total of 696 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Cell Biology and 4 papers in Immunology and Allergy. Recurrent topics in J. Philpot's work include Muscle Physiology and Disorders (15 papers), Cell Adhesion Molecules Research (4 papers) and Mitochondrial Function and Pathology (4 papers). J. Philpot is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Cell Adhesion Molecules Research (4 papers) and Mitochondrial Function and Pathology (4 papers). J. Philpot collaborates with scholars based in United Kingdom, Italy and Germany. J. Philpot's co-authors include Victor Dubowitz, Caroline A. Sewry, Francesco Muntoni, J.M. Pennock, Isam Naom, Graeme M. Bydder, Daniel Mahony, Leigh Wilson, Mariella D’Alessandro and Caroline King and has published in prestigious journals such as The Lancet, American Heart Journal and Archives of Disease in Childhood.

In The Last Decade

J. Philpot

15 papers receiving 684 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
J. Philpot United Kingdom	13	622	164	139	138	118	15	696
M. Chevallay France	15	415 0.7×	60 0.4×	99 0.7×	96 0.7×	59 0.5×	22	481
L. Feng United Kingdom	13	674 1.1×	51 0.3×	122 0.9×	254 1.8×	67 0.6×	19	795
F. Tomé France	11	507 0.8×	41 0.3×	59 0.4×	99 0.7×	83 0.7×	15	584
Andoni Urtizberea France	15	555 0.9×	39 0.2×	161 1.2×	129 0.9×	90 0.8×	27	796
Y. Sunada Japan	3	333 0.5×	76 0.5×	84 0.6×	56 0.4×	67 0.6×	4	364
Adnan Manzur United Kingdom	13	453 0.7×	30 0.2×	66 0.5×	133 1.0×	57 0.5×	37	588
Cíntia Yuri Matsumura Brazil	12	398 0.6×	27 0.2×	91 0.7×	61 0.4×	131 1.1×	22	510
Rita C.M. Pavanello Brazil	18	899 1.4×	16 0.1×	108 0.8×	254 1.8×	93 0.8×	50	1.0k
Laura Jarre Italy	12	291 0.5×	27 0.2×	46 0.3×	58 0.4×	28 0.2×	18	385
Alberto A. Zambon Italy	11	226 0.4×	43 0.3×	32 0.2×	60 0.4×	30 0.3×	26	324

Countries citing papers authored by J. Philpot

Since Specialization

Citations

This map shows the geographic impact of J. Philpot's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by J. Philpot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Philpot more than expected).

Fields of papers citing papers by J. Philpot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. Philpot. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by J. Philpot. The network helps show where J. Philpot may publish in the future.

Co-authorship network of co-authors of J. Philpot

This figure shows the co-authorship network connecting the top 25 collaborators of J. Philpot. A scholar is included among the top collaborators of J. Philpot based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J. Philpot. J. Philpot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Philpot, J., Serena J. Counsell, Graeme M. Bydder, et al.. (2001). Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?. Neuromuscular Disorders. 11(5). 489–493. 9 indexed citations

Philpot, J., J.M. Pennock, Frances M. Cowan, et al.. (2000). Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy. European Journal of Paediatric Neurology. 4(3). 109–114. 15 indexed citations

Mercuri, Eugenio, J. Philpot, Serena J. Counsell, et al.. (1999). Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status. Neuromuscular Disorders. 9(6-7). 383–387. 27 indexed citations

Philpot, J., et al.. (1999). Feeding problems in merosin deficient congenital muscular dystrophy. Archives of Disease in Childhood. 80(6). 542–547. 68 indexed citations

Philpot, J., Frances M. Cowan, J.M. Pennock, et al.. (1999). Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging. Neuromuscular Disorders. 9(2). 81–85. 83 indexed citations

Spyrou, Nicos, J. Philpot, Rodney A. Foale, P.G. Camici, & Francesco Muntoni. (1998). Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophy. American Heart Journal. 136(3). 474–476. 48 indexed citations

Naom, Isam, Mariella D’Alessandro, Caroline A. Sewry, et al.. (1998). Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy. Neuromuscular Disorders. 8(7). 495–501. 43 indexed citations

Philpot, J., et al.. (1997). Feeding problems in merosin-deficient congenital muscular dystrophy. Neuromuscular Disorders. 7(6-7). 433–433. 2 indexed citations

Naom, Isam, Mariella D’Alessandro, Haluk Topaloğlu, et al.. (1997). Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.. Journal of Medical Genetics. 34(2). 99–104. 33 indexed citations

10.

Sewry, Caroline A., J. Philpot, Isam Naom, et al.. (1996). Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy. The Lancet. 347(9001). 582–584. 52 indexed citations

11.

Mercuri, Eugenio, Lilly Dubowitz, Angela Berardinelli, et al.. (1995). Minor Neurological and Perceptuo-Motor Deficits in Children with Congenital Muscular Dystrophy: Correlation with Brain MRI Changes. Neuropediatrics. 26(3). 156–162. 14 indexed citations

12.

Mercuri, Eugenio, Francesco Muntoni, Angela Berardinelli, et al.. (1995). Somatosensory and Visual Evoked Potentials in Congenital Muscular Dystrophy: Correlation with MRI Changes and Muscle Merosin Status. Neuropediatrics. 26(1). 3–7. 49 indexed citations

13.

Philpot, J., Caroline A. Sewry, J.M. Pennock, & Victor Dubowitz. (1995). Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal. Neuromuscular Disorders. 5(4). 301–305. 137 indexed citations

14.

Sewry, Caroline A., J. Philpot, Daniel Mahony, et al.. (1995). Expression of laminin subunits in congenital muscular dystrophy. Neuromuscular Disorders. 5(4). 307–316. 92 indexed citations

15.

Philpot, J., Haluk Topaloğlu, J.M. Pennock, & Victor Dubowitz. (1995). Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy. Neuromuscular Disorders. 5(3). 227–231. 24 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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